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Medulloblastoma

Medulloblastoma (MB) is recognized as the most prevalent malignant brain tumor in pediatric patients, comprising approximately 25–30% of all childhood brain tumors. At Alfa Cytology, we are committed to pioneering new therapeutic approaches for medulloblastoma treatment for our clients.

Introduction to Medulloblastoma

Medulloblastoma originates in the cerebellum, specifically in the posterior fossa. The World Health Organization (WHO) classifies MB into four distinct molecular subtypes: WNT, Sonic Hedgehog (SHH), Group 3, and Group 4. Each subtype exhibits unique biological behaviors, prognostic outcomes, and therapeutic responses, making personalized treatment approaches essential.

Fig.1 Molecular features, prognosis, and location of the medulloblastoma subtypes. (Lombardi, G., et al., 2022)Fig.1 Molecular features, prognosis, and location of the medulloblastoma subtypes. (Lombardi, G., et al., 2022)

Recent advancements in molecular biology have illuminated the pathogenesis of these subtypes. For instance, WNT medulloblastomas typically feature mutations in the CTNNB1 gene, which encodes β-catenin, leading to the activation of WNT signaling pathways. In contrast, SHH medulloblastomas are associated with alterations in the PTCH1 and SUFU genes, highlighting the role of the Hedgehog signaling pathway in tumor development. Understanding these molecular underpinnings is crucial for developing targeted therapies that can improve clinical outcomes for affected children.

Therapeutic Development for Medulloblastoma

The therapeutic landscape for medulloblastoma has evolved significantly over the past decade. Traditional treatment modalities include surgical resection, radiotherapy, and chemotherapy. However, the advent of molecular profiling has paved the way for innovative therapeutic strategies tailored to the specific subtype of medulloblastoma.

NCT Target Therapeutics Phase
NCT04315064 Pan Histone Deacetylase (HDAC) Inhibitor MTX110
NCT04696029 Ornithine Decarboxylase Inhibitor Difluoromethylornithine (DFMO)
NCT01708174 Selective Smoothened Inhibitor LDE225
NCT03904862 Selective Inhibitor of CK2 (Casein Kinase 2) CX-4945
NCT01483820 Microtubule Inhibitor TPI 287
NCT01326104 Autologous Tumor-Specific T Cell Immunotherapy (TTRNA-xALT) Biological: TTRNA-xALT
NCT06161519 Topoisomerase I Inhibitor PLX038

Our Services

At Alfa Cytology, we are dedicated to advancing research and development in the field of medulloblastoma through our comprehensive preclinical services. Our expertise spans molecular profiling, in vivo and in vitro studies, biomarker discovery, and strategic consultation.

  • Cell Therapy
  • Gene Therapy
  • Oncolytic Virotherapy
  • Vaccine

Therapeutics Development

  • In Vivo PK
  • Safety Assessment

Contact Us

For more information about our services or to discuss potential collaborations, please contact us at Alfa Cytology. Our team is committed to driving innovation and improving treatment options for medulloblastoma.

Reference

  1. Fang, F.Y.; Rosenblum, J.S.; Ho, W.S.; Heiss, J.D. New Developments in the Pathogenesis, Therapeutic Targeting, and Treatment of Pediatric Medulloblastoma. Cancers 2022, 14, 2285. Lombardi, G.; et al. (2022). Diagnosis and Treatment of Pineal Region Tumors in Adults: A EURACAN Overview[J]. Cancers. 14, 3646.
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.